Product Recalls in Missouri
Product recalls affecting Missouri — including food, drugs, consumer products, medical devices, and vehicles distributed to Missouri. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,747 recalls have been distributed to Missouri in the last 12 months.
Showing 49341–49360 of 52,570 recalls
Recalled Item: See's Candies Recalled by See's Candies Inc. Due to One code of 1.7 oz...
The Issue: One code of 1.7 oz Divinity Easter Eggs with Walnuts may actually contain...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Vascular Solutions Recalled by Vascular Solutions, Inc. Due to Risk that air...
The Issue: Risk that air may be introduced into the device which may lead to an air...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Prostiva RF Therapy Generator. The Prostiva RF system is Recalled...
The Issue: Medtronic has found through device testing that if the optional footswitch...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The LifeCare PCA infusion system with Hospira MedNet software allows...
The Issue: The infusion pump has a clear plastic door that, due to its design, allows...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CDI Blood Parameter Monitoring System 500 with Arterial and Venous Recalled...
The Issue: Terumo discovered through its own testing that CDI 500 Blood Parameter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CDI Blood Parameter Monitoring System 500 with Venous blood parameter...
The Issue: Terumo discovered through its own testing that CDI 500 Blood Parameter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CDI Blood Parameter Monitoring System 500 with Arterial blood parameter...
The Issue: Terumo discovered through its own testing that CDI 500 Blood Parameter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CDI Blood Parameter Monitoring System 500 with Arterial and Venous Recalled...
The Issue: Terumo discovered through its own testing that CDI 500 Blood Parameter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nicolet EEG Wireless Amplifier 32/64 Channel. Catalog/Part Numbers :...
The Issue: Natus Neurology Incorporated is recalling the Nicolet EEG Wireless Amplifier...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sirtex SIR-yttrium 90 microspheres (Radionuclide) Recalled by Sirtex Medical...
The Issue: Incorrect expiration date
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The PCA 3 infusion pump allows clinicians Recalled by Hospira Inc. Due to...
The Issue: The infusion pump has a clear plastic door that, due to its design, allows...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CDI Blood Parameter Monitoring System 500 with Arterial blood parameter...
The Issue: Terumo discovered through its own testing that CDI 500 Blood Parameter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 0.9% Sodium Chloride Injection Recalled by Baxter Healthcare Corp. Due to...
The Issue: Labeling Wrong Barcode; It may display wrong product code 0.9% Sodium...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fenofibric Acid Recalled by Mutual Pharmaceutical Company, Inc. Due to...
The Issue: Labeling: Incorrect instructions; an error in section 5.11 of the patient...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: FIBRICOR (fenofibric acid) Tablets Recalled by Mutual Pharmaceutical...
The Issue: Labeling: Incorrect instructions; an error in section 5.11 of the patient...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fenofibric Acid Recalled by Mutual Pharmaceutical Company, Inc. Due to...
The Issue: Labeling: Incorrect instructions; an error in section 5.11 of the patient...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lisinopril Tablets Recalled by Mylan Pharmaceuticals Inc. Due to...
The Issue: Tablets/Capsules Imprinted With Wrong ID: Pharmaceuticals are imprinted with...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: QUELICIN (succinylcholine chloride) Injection Recalled by Hospira Inc. Due...
The Issue: Lack of Assurance of Sterility: Loose crimp applied to the fliptop vial.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sodium Acetate Injection Recalled by Hospira Inc. Due to Lack of Assurance...
The Issue: Lack of Assurance of Sterility: Loose crimp applied to the fliptop vial.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Furosemide Injection Recalled by Hospira Inc. Due to Lack of Assurance of...
The Issue: Lack of Assurance of Sterility: Loose crimp applied to the fliptop vial.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.